# K954678: Pro Vision

- Pathway: 510(k) (Traditional)
- Applicant: Algotec Systems, Ltd.
- Decided: Jan 5, 1996 after 87 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
679 later devices descend from it; 2 cite it directly.
1 of 680 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K980648: Pro Vision (1998), 672 descendants of its own
- K992654: Plug 'N View 3D, Version 1.0 (1999), 670 descendants of its own
- K020546: Fusion 7D (2002), 442 descendants of its own
- K022692: Voxelplus Pacs (2002), 252 descendants of its own
- K051528: Mevis Liveranalyser/Liverviewer Software (2005), 226 descendants of its own

Source page: https://510kreport.com/device/K954678
Methodology: https://510kreport.com/methodology